Yoga With and Without VR for Core, Balance, and Stress in University Students

NCT ID: NCT07310017

Last Updated: 2025-12-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

32 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-06-19

Study Completion Date

2026-01-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The present study aims to investigate the combined and comparative effects of yoga exercise performed with and without virtual reality (VR) support on stress levels, core stabilization, and balance in university students aged 18-30. Participants will be screened using validated stress assessment tools to ensure inclusion of individuals with moderate to high perceived stress. Eligible participants will then be randomly assigned to one of two groups:(1) a virtual reality yoga group (VRYG), in which yoga sessions are delivered through immersive VR environments with therapist-guided breathing and movement instruction; and (2) a Traditional Yoga Group (TYG), in which the same therapist will give the same breathing and movement instructions without VR.

Both groups will undergo 12 supervised sessions over a period of four weeks (three sessions per week, each lasting 30 minutes). The intervention protocol includes a structured series of yoga postures designed to target trunk stability, flexibility, and balance, along with breathing techniques such as diaphragmatic breathing and the 4-7-8 method to promote relaxation and stress reduction. The VR group will perform these exercise within calming, immersive virtual environments,while the control group will perform them in a quite,well-lit physical space.

Outcome measures will be collected at baseline and after completion of the intervention. Psychological stress will be evaluated using the Depression, anxiety, and stress scale (DASS-21) with a focus on the stress sub-scale.Physiological indicators, including heart rate and blood pressure will be recorded at rest. Core stabilization will be assessed through plank and side-plank endurance tests, while balance will be evaluated using both static (single-leg stance) and dynamic (Y-Balance Test) protocols. These measures will allow for a comprehensive analysis of the intervention's effects on both mental and physical domains of health.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Health-Related Behavior

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Mind-body intervention Immersive therapy Breathing exercise Relaxation

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Investigators

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Virtual Reality Yoga Group

Group Type EXPERIMENTAL

Yoga

Intervention Type OTHER

A structured yoga program designed to improve core stability, postura balance, and stress management. The traditional yoga sessions will focus on breathing control, static and dynamic postures, and progressive muscles engagements. Each session last 30 minutes it's supervised by a physiotherapist, and takes place in a quiet room to minimise external distractions.

Virtual Reality

Intervention Type OTHER

The VR environment will be created by the MetaQuest 2 which is a immersive virtual realty headset. During the application, the environment will be chosen by the participants among pre-decided virtual environments, such as forest or ocean. According to the environment, the objects around the participants will move with their sounds. The sounds will be only related to the environment like the bird sound, waterfall sound or the wave sound. There is no instruction in the environment.

Traditional Yoga Group

Group Type ACTIVE_COMPARATOR

Yoga

Intervention Type OTHER

A structured yoga program designed to improve core stability, postura balance, and stress management. The traditional yoga sessions will focus on breathing control, static and dynamic postures, and progressive muscles engagements. Each session last 30 minutes it's supervised by a physiotherapist, and takes place in a quiet room to minimise external distractions.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Yoga

A structured yoga program designed to improve core stability, postura balance, and stress management. The traditional yoga sessions will focus on breathing control, static and dynamic postures, and progressive muscles engagements. Each session last 30 minutes it's supervised by a physiotherapist, and takes place in a quiet room to minimise external distractions.

Intervention Type OTHER

Virtual Reality

The VR environment will be created by the MetaQuest 2 which is a immersive virtual realty headset. During the application, the environment will be chosen by the participants among pre-decided virtual environments, such as forest or ocean. According to the environment, the objects around the participants will move with their sounds. The sounds will be only related to the environment like the bird sound, waterfall sound or the wave sound. There is no instruction in the environment.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* University student aged 18-30
* Moderate-to-high perceived stress levels (DASS-21)
* No contraindications for yoga or VR use

Exclusion Criteria

* Diagnosed psychological conditions requiring treatment
* Musculoskeletal limitations that prevent participation
* Use of medications affecting stress
* Current participation in structured stress-reduction programs
Minimum Eligible Age

18 Years

Maximum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Istinye University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Çiçek Günday

Asst. Prof.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Dr. Öğr. Üyesi Çiçek Günday, Asst. Prof.

Role: PRINCIPAL_INVESTIGATOR

Istinye University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Fizyoterapi ve Rehabilitasyon Uygulama ve Araștırma Merkezi (İSÜFİZYOTEM)

Istanbul, Zeytinburnu, Turkey (Türkiye)

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Dr. Öğr. Üyesi Çiçek Günday, Asst. Prof

Role: CONTACT

Phone: +90 507 188 8848

Email: [email protected]

PT Lamia Nidal Naeem Matran, PT

Role: CONTACT

Phone: +90 552 711 2991

Email: [email protected]

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Nurgül Dürüstkan Elbsaşı, Asst. Prof

Role: primary

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

25-38

Identifier Type: -

Identifier Source: org_study_id